HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954791Generated: November 1, 2026
Trifluoroacetic acid → HCID 22082733, compound
https://huagongshe.com/reaction/1954791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 22082763 | HCID 22082763 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22082733 | HCID 22082733 | 70% |
Reaction Steps
To an ice-cooled solution of (R)-N-[8-(4-tert-butyloxycarbonylpiperazin-1-yl)-1,2,3,4 tetrahydro-2-naphthyl]-4-morpholinophenylcarboxamide (1.0 g, 2 mmol) in methylene chloride (100 mL) was added trifluoroacetic acid (3 mL). The reaction was stirred at ambient temperature for 7 h. The solvent was evaporated in vacuo and the residue was dissolved in water (20 mL), alkalized with a 2 M aqueous sodium hydroxide solution and extracted, twice, with methylene chloride. The phases were separated, the combined organic phases were dried (Na2SO4), filtered and evaporated in vacuo. Purification on a silica gel column using chloroform/methanol/concentrated ammonium hydroxide (95:5:0.5) as the eluent gave 580 mg (70% yield) of the title compound as white crystals: mp 202-203° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06124283 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-5b8fb6780460429baa4707ea19e1aff3 |
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| Source note | uspto-grants-2000_09 |
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